Other primary disorders of muscles digital illustration

Other primary disorders of muscles Save


ICD-10 code: G71.8

Chapter: Diseases of the nervous system

Other Primary Disorders of Muscles

When we think of muscle disorders, we often think of conditions like muscular dystrophy and myasthenia gravis. However, there are several other primary disorders of muscles that can cause significant impairments and disabilities. Here are some of the lesser-known primary muscle disorders:

  1. Mitochondrial Myopathies: These are a group of rare genetic disorders that affect the mitochondria, which are responsible for producing energy in the cells. Mitochondrial myopathies can cause muscle weakness, exercise intolerance, and fatigue. They can also affect other parts of the body, such as the eyes, ears, and brain.
  2. Nemaline Myopathy: This is a rare genetic disorder that causes muscle weakness and low muscle tone. It is caused by mutations in genes that regulate the structure and function of muscle fibers. Nemaline myopathy can affect both skeletal and smooth muscles, and can cause respiratory and feeding problems in severe cases.
  3. Congenital Myopathies: These are a group of genetic disorders that affect the structure and function of muscle fibers. Congenital myopathies can cause muscle weakness, low muscle tone, and delayed motor development. They can also affect other parts of the body, such as the heart and lungs.
  4. Familial Periodic Paralysis: This is a rare genetic disorder that causes episodes of muscle weakness or paralysis that come and go. It is caused by mutations in genes that regulate the flow of ions in and out of muscle cells. Familial periodic paralysis can be triggered by factors such as exercise, stress, or certain foods.
  5. Myotonia: This is a group of genetic disorders that cause muscle stiffness and difficulty relaxing the muscles after contraction. Myotonia can affect various parts of the body, such as the hands, face, and legs. It can also be triggered by factors such as cold temperatures, stress, or sudden movements.

If you or someone you know has symptoms of a primary muscle disorder, it is important to seek medical attention. A doctor can perform tests, such as muscle biopsies and genetic testing, to determine the underlying cause of the symptoms. Treatment options may include medications, physical therapy, and lifestyle modifications.

Overall, while primary muscle disorders may not be as well-known as some other conditions, they can still have a significant impact on a person's quality of life. By raising awareness of these disorders, we can help ensure that individuals with muscle disorders receive the care and support they need.

Diagnosis Codes for Other primary disorders of muscles | G71.8